PE20030269A1 - Derivados de benzamida tiazol y composiciones farmaceuticas para inhibir la proliferacion de celulas - Google Patents
Derivados de benzamida tiazol y composiciones farmaceuticas para inhibir la proliferacion de celulasInfo
- Publication number
- PE20030269A1 PE20030269A1 PE2002000595A PE2002000595A PE20030269A1 PE 20030269 A1 PE20030269 A1 PE 20030269A1 PE 2002000595 A PE2002000595 A PE 2002000595A PE 2002000595 A PE2002000595 A PE 2002000595A PE 20030269 A1 PE20030269 A1 PE 20030269A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- benzamide
- ilamine
- heteroalkyl
- haloalkyl
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P13/12—Drugs for disorders of the urinary system of the kidneys
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D277/38—Nitrogen atoms
- C07D277/42—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Virology (AREA)
- Immunology (AREA)
- Oncology (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Communicable Diseases (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Molecular Biology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Dermatology (AREA)
- Urology & Nephrology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pain & Pain Management (AREA)
- Biotechnology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Psychiatry (AREA)
- Vascular Medicine (AREA)
- AIDS & HIV (AREA)
- Endocrinology (AREA)
- Psychology (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US30367901P | 2001-07-06 | 2001-07-06 | |
US30527401P | 2001-07-13 | 2001-07-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20030269A1 true PE20030269A1 (es) | 2003-04-16 |
Family
ID=26973595
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2002000595A PE20030269A1 (es) | 2001-07-06 | 2002-07-02 | Derivados de benzamida tiazol y composiciones farmaceuticas para inhibir la proliferacion de celulas |
Country Status (13)
Country | Link |
---|---|
US (1) | US6720346B2 (ja) |
EP (1) | EP1438046A4 (ja) |
JP (1) | JP2005521631A (ja) |
AU (1) | AU2002354801A1 (ja) |
BR (1) | BR0210874A (ja) |
CA (1) | CA2452609A1 (ja) |
HN (1) | HN2002000156A (ja) |
MX (1) | MXPA04000069A (ja) |
PA (1) | PA8550101A1 (ja) |
PE (1) | PE20030269A1 (ja) |
SV (1) | SV2003001148A (ja) |
UY (1) | UY27370A1 (ja) |
WO (1) | WO2003004467A2 (ja) |
Families Citing this family (33)
Publication number | Priority date | Publication date | Assignee | Title |
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US6495550B2 (en) * | 1999-08-04 | 2002-12-17 | Icagen, Inc. | Pyridine-substituted benzanilides as potassium ion channel openers |
DE60037321D1 (de) | 1999-08-04 | 2008-01-17 | Icagen Inc | Benzanilide als öffner des kaliumkanals |
US7705120B2 (en) | 2001-06-21 | 2010-04-27 | Millennium Pharmaceuticals, Inc. | Compositions, kits, and methods for identification, assessment, prevention, and therapy of breast cancer |
AU2003282231A1 (en) * | 2002-08-09 | 2004-02-25 | Pfizer Inc. | Antiproliferative 2-(heteroaryl)-aminothiazole compounds, pharmaceutical compositions and methods for their use |
DE602004028907D1 (de) * | 2003-02-06 | 2010-10-14 | Bristol Myers Squibb Co | Als kinaseinhibitoren geeignete verbindungen auf thiazolylbasis |
US7265138B2 (en) | 2003-02-10 | 2007-09-04 | Amgen Inc. | Vanilloid receptor ligands and their use in treatments |
WO2004072070A1 (en) * | 2003-02-12 | 2004-08-26 | Pfizer Inc. | Antiproliferative 2-(sulfo-phenyl)-aminothiazole derivatives |
US7652044B2 (en) * | 2003-06-03 | 2010-01-26 | Novartis A.G. | P-38 inhibitors |
ATE517872T1 (de) | 2003-06-26 | 2011-08-15 | Novartis Ag | Fünfgliedrige p38-kinaseinhibitoren auf heterocyclusbasis |
US20050026966A1 (en) * | 2003-07-30 | 2005-02-03 | Agouron Pharmaceuticals, Inc. | Process and chiral amine intermediates useful for preparation of antiproliferative 2,4-diaminothiazole amide compounds |
US20050164300A1 (en) * | 2003-09-15 | 2005-07-28 | Plexxikon, Inc. | Molecular scaffolds for kinase ligand development |
WO2005073225A1 (en) * | 2004-01-30 | 2005-08-11 | Ab Science | 2-(3-substituted-aryl)amino-4-aryl-thiazoles as tyrosine kinase inhibitors |
JP2007531773A (ja) | 2004-03-31 | 2007-11-08 | レキシコン・ジェネティクス・インコーポレーテッド | プロテインキナーゼ変調剤としての2−アミノメチルチアゾール−5−カルボキサミド |
WO2005102326A2 (en) * | 2004-04-23 | 2005-11-03 | Ab Science | Use of c-kit inhibitors for treating renal diseases |
US7618981B2 (en) * | 2004-05-06 | 2009-11-17 | Cytokinetics, Inc. | Imidazopyridinyl-benzamide anti-cancer agents |
US7423053B2 (en) * | 2004-07-15 | 2008-09-09 | Hoffmann-La Roche Inc. | 4-Aminothiazole derivatives |
JP4652079B2 (ja) * | 2005-02-15 | 2011-03-16 | 花王株式会社 | 2,2−二置換エチレンジアミン誘導体の製造方法 |
CA2600869A1 (en) | 2005-03-18 | 2006-09-28 | The Regents Of The University Of California | Compounds having activity in correcting mutant-cftr processing and uses thereof |
NZ563866A (en) | 2005-05-09 | 2011-03-31 | Achillion Pharmaceuticals Inc | Thiazole compounds and methods of use |
MX2008011791A (es) | 2006-03-15 | 2008-09-25 | Wyeth Corp | Azaciclilaminas-n-sustituidas como antagonistas de histamina-3. |
PE20080371A1 (es) | 2006-05-19 | 2008-04-09 | Wyeth Corp | N-benzoil-y-n-bencilpirrolidin-3-ilaminas como antagonistas de histamina-3 |
PE20081152A1 (es) | 2006-10-06 | 2008-08-10 | Wyeth Corp | Azaciclilaminas n-sustituidas como antagonistas de histamina-3 |
WO2008061923A1 (en) * | 2006-11-23 | 2008-05-29 | Ciba Holding Inc. | Process for the preparation of tertiary n-allyl sterically hindered amines |
JP5362585B2 (ja) * | 2007-01-31 | 2013-12-11 | チバ ホールディング インコーポレーテッド | カチオン性染料 |
GB0705656D0 (en) * | 2007-03-23 | 2007-05-02 | Addex Pharmaceuticals Sa | Novel compounds E1 |
WO2009012252A1 (en) | 2007-07-16 | 2009-01-22 | Wyeth | Aminoalkylazole derivatives as histamine-3 antagonists |
US9066951B2 (en) * | 2008-05-29 | 2015-06-30 | Wisconsin Alumni Research Foundation | Drugs to treat HPV infection |
CN102307882B (zh) * | 2008-12-03 | 2015-06-10 | 斯克里普斯研究所 | 干细胞培养 |
JP5212656B2 (ja) * | 2009-09-02 | 2013-06-19 | 日産化学工業株式会社 | イソチオシアナト化合物の製造方法 |
EP2647623A4 (en) | 2010-11-29 | 2015-12-30 | Nissan Chemical Ind Ltd | METHOD FOR PRODUCING AN ISOTHIOCYANATE COMPOUND |
WO2013089689A1 (en) * | 2011-12-13 | 2013-06-20 | Kneller Bruce W | Constituent of desmodium elegans and methods of use |
WO2015199206A1 (ja) * | 2014-06-27 | 2015-12-30 | 塩野義製薬株式会社 | Trpv4阻害活性を有する6員環誘導体 |
JP2020512976A (ja) * | 2017-03-27 | 2020-04-30 | ファーマケア,インク. | アポトーシスシグナル調節キナーゼ1(ask1)阻害剤化合物 |
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JPH10509708A (ja) | 1994-11-10 | 1998-09-22 | コア セラピューティクス,インコーポレイティド | プロテイン・キナーゼのインヒビターとして有用な医薬ピラゾール組成物 |
JP3884477B2 (ja) | 1995-03-22 | 2007-02-21 | 大正製薬株式会社 | チアゾール誘導体 |
DE69734149T2 (de) | 1996-03-15 | 2006-07-06 | Astrazeneca Ab | Cinoline derivate und verwendung als heilmittel |
TW513418B (en) | 1996-07-31 | 2002-12-11 | Otsuka Pharma Co Ltd | Thiazole derivatives, their production and use |
ATE332896T1 (de) * | 1997-10-27 | 2006-08-15 | Agouron Pharma | 4-aminothiazol derivate, deren herstellung und deren verwendung als inhibitoren cyclin- abhängiger kinasen |
CN1290165A (zh) | 1997-11-10 | 2001-04-04 | 布里斯托尔-迈尔斯斯奎布公司 | 苯并噻唑蛋白酪氨酸激酶抑制剂 |
US6040321A (en) | 1997-11-12 | 2000-03-21 | Bristol-Myers Squibb Company | Aminothiazole inhibitors of cyclin dependent kinases |
UA60365C2 (uk) | 1998-06-04 | 2003-10-15 | Пфайзер Продактс Інк. | Похідні ізотіазолу, спосіб їх одержання, фармацевтична композиція та спосіб лікування гіперпроліферативного захворювання у ссавця |
FR2780058B1 (fr) | 1998-06-17 | 2001-03-09 | Rhodia Chimie Sa | Emulsion aqueuse de silane pour l'hydrofugation de materiaux de construction |
JP2002526482A (ja) | 1998-09-18 | 2002-08-20 | バーテックス ファーマシューティカルズ インコーポレイテッド | p38のインヒビター |
GB9823873D0 (en) | 1998-10-30 | 1998-12-30 | Pharmacia & Upjohn Spa | 2-ureido-thiazole derivatives,process for their preparation,and their use as antitumour agents |
GB9823871D0 (en) | 1998-10-30 | 1998-12-23 | Pharmacia & Upjohn Spa | 2-Amino-thiazole derivatives, process for their preparation, and their use as antitumour agents |
US6756374B2 (en) | 2001-01-22 | 2004-06-29 | Hoffmann-La Roche Inc. | Diaminothiazoles having antiproliferative activity |
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2002
- 2002-06-26 HN HN2002000156A patent/HN2002000156A/es unknown
- 2002-07-02 PE PE2002000595A patent/PE20030269A1/es not_active Application Discontinuation
- 2002-07-04 UY UY27370A patent/UY27370A1/es not_active Application Discontinuation
- 2002-07-04 SV SV2002001148A patent/SV2003001148A/es not_active Application Discontinuation
- 2002-07-05 CA CA002452609A patent/CA2452609A1/en not_active Abandoned
- 2002-07-05 US US10/190,219 patent/US6720346B2/en not_active Expired - Fee Related
- 2002-07-05 WO PCT/US2002/021280 patent/WO2003004467A2/en active Application Filing
- 2002-07-05 EP EP02782499A patent/EP1438046A4/en not_active Withdrawn
- 2002-07-05 MX MXPA04000069A patent/MXPA04000069A/es unknown
- 2002-07-05 AU AU2002354801A patent/AU2002354801A1/en not_active Abandoned
- 2002-07-05 JP JP2003510635A patent/JP2005521631A/ja not_active Withdrawn
- 2002-07-05 BR BRPI0210874-7A patent/BR0210874A/pt not_active IP Right Cessation
- 2002-07-08 PA PA20028550101A patent/PA8550101A1/es unknown
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WO2003004467A2 (en) | 2003-01-16 |
PA8550101A1 (es) | 2003-09-05 |
BR0210874A (pt) | 2006-10-24 |
US20030225147A1 (en) | 2003-12-04 |
HN2002000156A (es) | 2003-11-27 |
CA2452609A1 (en) | 2003-01-16 |
SV2003001148A (es) | 2003-03-18 |
AU2002354801A1 (en) | 2003-01-21 |
EP1438046A4 (en) | 2004-10-20 |
MXPA04000069A (es) | 2004-05-21 |
US6720346B2 (en) | 2004-04-13 |
UY27370A1 (es) | 2003-04-30 |
JP2005521631A (ja) | 2005-07-21 |
EP1438046A2 (en) | 2004-07-21 |
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